Human Pathology
Volume 41, Issue 3 , Pages 385-391, March 2010

Abnormal expression of telomerase/apoptosis limits type II alveolar epithelial cell replication in the early remodeling of usual interstitial pneumonia/idiopathic pulmonary fibrosis

  • Daniel Reis Waisberg, MD

      Affiliations

    • Departament of Pathology, Faculdade de Medicina da Universidade de São Paulo, Brasil
  • ,
  • João Valente Barbas-Filho, MD, PhD

      Affiliations

    • Division of Respiratory Diseases of Instituto do Coração (InCor), Faculdade de Medicina da Universidade de São Paulo, Brasil
  • ,
  • Edwin Roger Parra, MD, PhD

      Affiliations

    • Departament of Pathology, Faculdade de Medicina da Universidade de São Paulo, Brasil
  • ,
  • Sandra Fernezlian, BS

      Affiliations

    • Departament of Pathology, Faculdade de Medicina da Universidade de São Paulo, Brasil
  • ,
  • Carlos Roberto Ribeiro de Carvalho, MD, PhD

      Affiliations

    • Division of Respiratory Diseases of Instituto do Coração (InCor), Faculdade de Medicina da Universidade de São Paulo, Brasil
  • ,
  • Ronaldo Adib Kairalla, MD, PhD

      Affiliations

    • Division of Respiratory Diseases of Instituto do Coração (InCor), Faculdade de Medicina da Universidade de São Paulo, Brasil
  • ,
  • Vera Luiza Capelozzi, MD, PhD

      Affiliations

    • Departament of Pathology, Faculdade de Medicina da Universidade de São Paulo, Brasil
    • Corresponding Author InformationCorresponding author. Faculdade de Medicina da Universidade de São Paulo, Departamento de Patologia, CEP 01296-903, São Paulo, SP, Brasil.

Received 2 July 2009; received in revised form 21 August 2009; accepted 26 August 2009. published online 02 December 2009.

Summary 

Idiopathic pulmonary fibrosis is a distinctive, usually fatal, type of chronic fibrosing interstitial pneumonia of unknown cause that increases in prevalence with advanced age, characterized by failure of alveolar re-epithelization and progressive scar formation. Recently, limitation of the replicative capacity of tissues determined by telomerase/apoptosis balance has been implicated in pathogenesis of age-related diseases. In this study, we validated the importance of the expression of type 2 alveolar epithelial cells telomerase protein and studied the relationships between telomerase and apoptosis in early remodeling of usual interstitial pneumonia. We determined type 2 alveolar epithelial cells density, telomerase expression, and apoptosis in surgical lung biopsies from 24 patients with usual interstitial pneumonia, and in normal lung tissues from 18 subjects. We used immunohistochemistry, deoxynucleotidyl transferase method of end labeling, electron microscopy, and histomorphometry to evaluate the amount of type 2 alveolar epithelial cells staining for surfactant-A, telomerase, and in situ detection of apoptotic cells. Unaffected areas of usual interstitial pneumonia and normal lung tissue had similar densities of type 2 alveolar epithelial cells, but a significant minor subpopulation of type 2 alveolar epithelial cells was telomerase positive and a large population was telomerase negative. A significant inverse association was found between low type 2 alveolar epithelial cell telomerase expression and high apoptosis in unaffected areas of usual interstitial pneumonia. Although type 2 alveolar epithelial cell telomerase expression was higher than apoptosis in NLT group, no significant association was found between them. Electron microscopy confirmed epithelial apoptosis, alveolar collapse, and initial fibroplasia. We conclude that abnormal type 2 alveolar epithelial cells telomerase/apoptosis balance may reduce alveolar epithelial regenerative capacity, thus contributing to the early remodeling response in usual interstitial pneumonia.

Keywords: Alveolar collapse, Apoptosis, Idiopathic pulmonary fibrosis, Prognosis, Telomerase, Type II alveolar epithelial cells

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 This study was supported by the following Brazilian agencies: the National Council for Scientific and Technological Development, the Foundation for the Support of Research of the State of São Paulo, and the Laboratories for Medical Research, Hospital das Clinicas, Faculdade de Medicina da Universidade de São Paulo.

PII: S0046-8177(09)00320-7

doi:10.1016/j.humpath.2009.08.019

Human Pathology
Volume 41, Issue 3 , Pages 385-391, March 2010